Description
This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.

Specification
Aliases	AKU; HGO
Swissprot	Q93099
WB Predicted band size	50 kDa
Host/Isotype	Rabbit IgG
Antibody Type	Primary antibody
Storage	Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity	Human, Mouse, Rat
Immunogen	Fusion protein of human HGD
Formulation	Purified antibody in PBS with 0.05% sodium azide and 50% glycerol.

Application
WB	1/500-1/2000
ELISA	1/5000-1/10000